Oral vaccination with inactivated influenza vaccine induces cross-protective immunity

被引:28
|
作者
Quan, Fu-Shi [1 ,2 ]
Compans, Richard W. [1 ]
Kang, Sang-Moo [1 ,3 ,4 ]
机构
[1] Emory Univ, Sch Med, Dept Microbiol & Immunol, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[2] Chungju Natl Univ, Dept Biotechnol, Jeungpyeong 368701, South Korea
[3] Georgia State Univ, Dept Biol, Atlanta, GA 30303 USA
[4] Georgia State Univ, Ctr Inflammat Immun & Infect, Dept Biol, Atlanta, GA 30303 USA
关键词
Influenza; Oral vaccination; Cross protection; VIRUS-LIKE PARTICLES; LIVE ATTENUATED VIRUSES; HEAT-LABILE ENTEROTOXIN; ESCHERICHIA-COLI; HETEROSUBTYPIC IMMUNITY; DENDRITIC CELLS; IMMUNIZATION; DELIVERY; RESPONSES; MICE;
D O I
10.1016/j.vaccine.2011.11.028
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Oral vaccination would provide an easy and safe measure to prevent infectious diseases by facilitating mass immunization. We investigated the feasibility of oral vaccination with inactivated whole influenza virus (A/PR8/34). Oral vaccination of mice induced high levels of serum IgG and IgA antibodies specific to the homologous virus (A/PR8) as well as cross reactive to heterologous (A/California/04/09) and heterosubtypic viruses (A/Philippines/2/82). IgG1 isotype antibodies were found to be induced at significantly higher levels than IgG2a antibodies. These antibodies induced by oral vaccination exhibited hemagglutination inhibition activities. High levels of both IgG and IgA antibodies were induced in vagina and lungs. Mucosal IgA antibodies were also elicited in other sites including saliva, urine, and fecal samples. Orally vaccinated mice were completely protected against challenge with homologous or heterologous viruses, and partially protected against heterosubtypic virus. Importantly, high recall antibody secreting cell (ASC) responses were induced in spleen, indicating the generation of memory B cells by oral vaccination. The present study therefore presents new findings of cross-reactive antibodies at systemic and diverse mucosal sites, recall antibody responses, and cross-protective efficacies by oral vaccination, thus supporting a proof-of-concept that oral delivery of vaccines can be developed as an effective vaccination route. (C) 2011 Published by Elsevier Ltd.
引用
收藏
页码:180 / 188
页数:9
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